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J Mol Biol. 1999 Dec 17;294(5):1351-62.

Sequence and structure-based prediction of eukaryotic protein phosphorylation sites.

Author information

1
Department of Biotechnology, The Technical University of Denmark, Lyngby, DK-2800, Denmark.

Abstract

Protein phosphorylation at serine, threonine or tyrosine residues affects a multitude of cellular signaling processes. How is specificity in substrate recognition and phosphorylation by protein kinases achieved? Here, we present an artificial neural network method that predicts phosphorylation sites in independent sequences with a sensitivity in the range from 69 % to 96 %. As an example, we predict novel phosphorylation sites in the p300/CBP protein that may regulate interaction with transcription factors and histone acetyltransferase activity. In addition, serine and threonine residues in p300/CBP that can be modified by O-linked glycosylation with N-acetylglucosamine are identified. Glycosylation may prevent phosphorylation at these sites, a mechanism named yin-yang regulation. The prediction server is available on the Internet at http://www.cbs.dtu.dk/services/NetPhos/or via e-mail to NetPhos@cbs. dtu.dk.

PMID:
10600390
DOI:
10.1006/jmbi.1999.3310
[Indexed for MEDLINE]

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